{{Rsnum
|rsid = 28936686
|Gene = CAV3
|geno1 = (A;A)
|geno2 = (A;G)
|geno3 = (G;G)
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|Chromosome=3
|position=8745688
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CAV3,SSUH2
}}{{omim
|desc=RIPPLING MUSCLE DISEASE 2, AUTOSOMAL RECESSIVE
|id=601253
|rsnum=28936686
|variant=0010
}}
{{ neighbor
| rsid = 28936685
| distance = 17
}}

{{ClinVar
|rsid=28936686
|Reversed=0
|FwdREF=G
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=8787374
|CHROM=3
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=CAV3:859
|GENE_NAME=CAV3
|GENE_ID=859
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.8787374G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000008780.1; RCV000024388.1
|CLNDBN=Rippling muscle disease 2, autosomal recessive; not provided
|CLNSRC=Leiden Muscular Dystrophy pages (CAV3); OMIM Allelic Variant
|CLNSRCID=CAV3_00012; 601253.0010
|Disease=Rippling muscle disease 2; not provided
}}

{{PMID Auto
|PMID=15668980
|Title=Autosomal recessive rippling muscle disease with homozygous CAV3 mutations.
}}

{{PMID Auto
|PMID=12666119
|Title=Homozygous mutations in caveolin-3 cause a severe form of rippling muscle disease.
}}

{{PMID Auto
|PMID=19697367
|Title=Rippling muscle disease: variable phenotype in a family with five afflicted members.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}